IP Library Granted Patent US 9,364,556
Granted Patent B2
US 9,364,556 · App. 14/360,937 · Granted Jun 14, 2016

Drug conjugate comprising drug linked to human c-Met antibody, and use therefor

Inventors: Young Woo Park (Daejeon, KR); Ki Won Jo (Daejeon, KR); Sun Jeong Jo (Daejeon, KR); Soon Sil Hyun (Daejeon, KR); Jae Eun Park (Daejeon, KR); Seok Ho Yoo (Daejeon, KR); Myeoung Hee Jang (Daejeon, KR); Hye Nan Kim (Daejeon, KR); Chan Woong Park (Gwangju, KR)
Assignees: Korea Research Institute of Bioscience and Biotechnology; A&RT Co., Ltd.
A61K47/48407A61K31/704A61K47/48561C07K16/2803C07K16/2863A61K2039/505
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Quick Facts
Patent No.
US 9,364,556
App. No.
14/360,937
Granted
Jun 14, 2016
Kind
B2
Abstract

The present invention relates to a drug conjugate comprising a cytotoxic drug conjugated to a c-Met specific human antibody. More specifically, the present invention relates to: a drug conjugate comprising a cytotoxic drug conjugated to a c-Met specific human antibody; a pharmaceutical composition for cancer treatment comprising the drug conjugate; and a cancer treatment method comprising a step in which the drug conjugate or pharmaceutical composition is administered to an individual.

Claims (24)

1. An antibody-drug conjugate comprising a cytotoxic, drug conjugated to a c-Met-specific human antibody, wherein the antibody comprises:

a heavy-chain variable region comprising:

i) a heavy-chain CDR1 comprising amino acids having the sequence set forth it SEQ ID NO: 1;

ii) a heavy-chain CDR2 comprising amino acids having the sequence set forth in SEQ ID NO: 2; and

iii) a heavy-chain CDR3 comprising amino acids having the sequence set forth SEQ ID NO: 3; and

a light-chain variable region comprising:

i) a light-chain CDR1 comprising amino acids having the sequence set forth in SEQ ID NO: 4;

ii) a light-chain CDR2 comprising amino acids having the sequence set forth in SEQ ID NO: 5; and

iii) a light-chain CDR3 comprising amino acids having the sequence set forth in SEQ ID NO: 6.

2. The antibody-drug conjugate of claim 1 , wherein the heavy-chain variable region of the human antibody further comprises cysteine.

3. The antibody-drug conjugate of claim 1 , wherein the human antibody is an agonistic antibody against c-Met.

4. The antibody-drug conjugate of claim 1 , wherein the human antibody comprises a heavy-chain variable region comprising amino acids having the sequence set forth in SEQ ID NO: 7 or 8 and a light-chain variable region comprising amino acids having the sequence set forth in SEQ ID NO: 11.

5. The antibody-drug conjugate of claim 1 , wherein the human antibody comprises a heavy-chain constant region comprising amino acids having the sequence set forth in SEQ ID NO: 13 and a light-chain constant region comprising amino acids having the sequence set forth in SEQ ID NO: 15.

6. The antibody-drug conjugate of claim 1 , wherein the cytotoxic, drug is conjugated to the human antibody by a linker.

7. The antibody-drug conjugate of claim 6 , wherein the linker is a hydrazone or a peptide linker.

8. The antibody-drug conjugate of claim 1 , wherein the cytotoxic drug is conjugated to the human antibody by a Schiff base.

9. The antibody-drug conjugate of claim 6 , wherein the cytotoxic drug is conjugated to the human antibody by [linker-Val (valine)-Cit (citrulline)] or [linker-Schiff base].

10. The antibody-drug conjugate of claim 1 , wherein the cytotoxic drug is selected from the group consisting of doxorubicin, carboplatin (paraplatin), cisplatin, cyclophosphamide, ifosfamide, nidran, nitrogen mustard (mechlorethamine HCL), Neomycin, mitomycin C, cytarabine, flurouracil, gemcitabine, trimetrexate, methotrexate, etoposide, vinblastine, vinorelbine, alimta, altretamine, procarbazine, taxol, taxotere, topotecan and irinotecan.

11. A pharmaceutical composition for treating cancer that expresses c-Met, which comprises the antibody-drug conjugate of claim 1 .

12. The pharmaceutical composition of claim 11 , wherein the cancer is a hypoxic tumor.

13. The pharmaceutical composition of claim 11 , wherein the conjugate is internalized into cells by endocytosis.

14. The pharmaceutical composition of claim 11 , wherein the cytotoxic drug of the conjugate is separated either by intracellular protease or under an intracellular acidic condition.

15. A method for treating cancer that expresses c-Met, which comprises administering the antibody-drug, conjugate of claim 1 to a subject.

16. A method for treating cancer that expresses c-Met, which comprises administering the pharmaceutical composition of claim 11 to a subject.

Assignments (3)
CHANGE OF NAME Recorded Jan 18, 2016
From: A&R THERAPEUTICS CO., LTD.
To: A&RT CO., LTD.
Reel/Frame 037550/0045 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Sep 29, 2014
From: PARK, YOUNG WOO; JO, KI WON; JO, SUN JEONG; HYUN, SOON SIL; PARK, CHAN WOONG
To: KOREA RESEARCH INSTITUTE OF BIOSCIENCE AND BIOTECHNOLOGY
Reel/Frame 033835/0199 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Sep 29, 2014
From: PARK, JAE EUN; YOO, SEOK HO; JANG, MYEOUNG HEE; KIM, HYE NAN
To: A&R THERAPEUTICS CO., LTD.
Reel/Frame 033835/0203 →
Priority Claims (1)
KR 10-2011-0125255 · Nov 28, 2011 · national
Continuity (1)
Related Publication 20150110815A1 · Apr 23, 2015